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Conmed

FDA UDI

Class I (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
CONMED FDA UDI
Generic Name
Bone/joint surgical power tool motorized handpiece/set, pneumatic FDA UDI
Device Name
STERNUM SAW HANDPIECE FDA UDI
Model / Reference
00505900500 FDA UDI
Description
STERNUM SAW HANDPIECE FDA UDI

Identifiers

Catalog Number
5056-005 FDA UDI
Primary DI / UDI-DI
20845854013219 FDA UDI
FDA Product Code
KFK FDA UDI
GMDN Term
Bone/joint surgical power tool motorized handpiece/set, pneumatic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone/joint surgical power tool motorized handpiece/set, pneumatic

Conmed by Conmed Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone/joint surgical power tool motorized handpiece/set, pneumatic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 9d009768-25f3-4f6e-b8b1-f41309379962 36 fields · synced May 30, 2026